| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs112445441 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 32 | |||
| rs121913227 | 0.653 | 0.320 | 7 | 140753336 | missense variant | AC/CT;TT | mnv | 31 | |||
| rs36053993 | 0.677 | 0.280 | 1 | 45331556 | missense variant | C/T | snv | 3.0E-03 | 3.3E-03 | 31 | |
| rs777980327 | 0.716 | 0.280 | 5 | 112837567 | missense variant | A/T | snv | 4.0E-06 | 7.0E-06 | 21 | |
| rs2228612 | 0.763 | 0.160 | 19 | 10162696 | missense variant | T/A;C;G | snv | 0.14 | 12 | ||
| rs121913341 | 0.851 | 0.280 | 7 | 140753350 | missense variant | A/C;T | snv | 5 | |||
| rs910532454 | 0.882 | 0.080 | 2 | 136115453 | missense variant | C/A;T | snv | 4.0E-06 | 4 | ||
| rs147198552 | 0.882 | 0.080 | 2 | 136115450 | missense variant | C/T | snv | 1.2E-05 | 7.0E-06 | 3 |